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Structure of 52718-95-3
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Methyl 2-bromonicotinate is a bench-stable, moisture-tolerant brominated pyridine derivative featuring a strategically positioned ester group. This compound integrates readily into cross-coupling reactions and serves as a key intermediate for synthesizing bioactive heterocycles and functionalized pharmaceuticals.
Methyl 2-bromonicotinate serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the pyridine ring via palladium-catalyzed cross-coupling reactions. Its bromo group exhibits high reactivity in Suzuki, Stille, and Negishi couplings, while the methyl ester facilitates selective derivatization. The compound demonstrates excellent bench stability and compatibility with diverse reaction conditions, making it ideal for constructing complex heterocyclic scaffolds and pharmaceutical intermediates.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: